Visitor Monitoring Drug History: SINOGRAFIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: SINOGRAFIN
FDA Application No: (NDA) 011324
Active Ingredient(s): DIATRIZOATE MEGLUMINE; IODIPAMIDE MEGLUMINE
Company: BRACCO
 
Label History
 
Labels are not available on this site for SINOGRAFIN, (NDA) 011324
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
3/16/2000 030Manufacturing Change or Addition  
4/29/1994 029Control Supplement  
4/17/2002 028Labeling Revision Letter 
1/28/1985 027Manufacturing Change or Addition  
8/6/1985 025Manufacturing Change or Addition  
6/3/1983 024Control Supplement  
8/3/1983 023Control Supplement  
7/22/1983 022Practioner Draft Labeling  
7/11/1979 021Package Change  
6/26/1979 020Labeling Revision  
2/15/1979 019Control Supplement  
12/28/1978 018Control Supplement  
12/28/1978 017Formulation Revision  
5/31/1978 016Control Supplement  
9/25/1978 015Control Supplement  
2/15/1979 014Control Supplement  
4/4/1977 013Control Supplement  
1/11/1977 011Control Supplement  
5/31/1978 010Labeling Revision  
5/5/1976 009Control Supplement  
9/25/1975 008Control Supplement  
5/29/1975 007Control Supplement  
8/22/1958 000Approval  
 
There are no Therapeutic Equivalents
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